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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187425Generated: November 2, 2026

Hydrazine → HCID 68539374, compound

https://huagongshe.com/reaction/1187425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
ReactantHCID 68539763HCID 68539763—
SolventEthanolHCID 702—
ProductHCID 68539374HCID 68539374135%

Reaction Steps

Anhydrous hydrazine (94 mg, 2.96 mmol) was added to 2-[4-(4-amino-6,7,8,9-tetrahydro-1H-imidazo[4,5-c]quinolin-1-yl)butoxy]-1H-isoindole-1,3(2H)-dione (600 mg, 1.48 mmol) in ethanol (25 mL) at ambient temperature. The reaction was stirred overnight, and additional hydrazine (2 equivalents) was added. After sting for 2 hours at ambient temperature, the reaction was concentrated under reduced pressure. The residue was diluted with dichloromethane and concentrated under reduced pressure three times to remove the hydrazine and then dried under vacuum to provide 550 mg of impure 1-[4-(aminooxy)butyl]-6,7,8,9-tetrahydro-1H-imidazo[4,5-c]quinolin4-amine as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673932B2
Source datasetuspto-grants-2014_03
ORD IDord-d8aab179250049069e08957606f36398
Source noteuspto-grants-2014_03